Student Research Committee, Department of Food Science and Technology, Faculty of Nutrition and Food Science, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran, Iran.
Adv Colloid Interface Sci. 2020 Apr;278:102125. doi: 10.1016/j.cis.2020.102125. Epub 2020 Feb 19.
The genesis of dendrimers can be considered as a revolution in nano-scaled bioactive delivery systems. These structures possess a unique potential in encapsulating/entrapping bioactive ingredients due to their tree-like nature. Therefore, they could swiftly obtain a valuable statue in nutraceutical, pharmaceutical and medical sciences. Phytochemicals, as a large proportion of bioactives, have been studied and used by scholars in several fields of pharmacology, medical, food, and cosmetic for many years. But, the solubility, stability, and bioavailability issues have always been recognized as limiting factors in their application. Therefore, the main aim of this study is representing the use of dendrimers as novel nanocarriers for phytochemical bioactive compounds to deal with these problems. Hence, after a brief review of phytochemical ingredients, the text is commenced with a detailed explanation of dendrimers, including definitions, types, generations, synthesizing methods, and safety issues; then is continued with demonstration of their applications in encapsulation of phytochemical bioactive compounds and their active/passive delivery by dendrimers. Dendrimers provide a vast and appropriate surface to entrap the targeted phytochemical bioactive ingredients. Several parameters can affect the yield of nanoencapsulation by dendrimers, including their generation, type of end groups, surface charge, core structure, pH, and ambient factors. Another important issue of dendrimers is related to their toxicity. Cationic dendrimers, particularly PAMAM can be toxic to body cells through attaching to the cell membranes and disturbing their functions. However, a number of solutions have been suggested to decrease their toxicity.
树状聚合物的起源可以被认为是纳米级生物活性递药系统的一场革命。由于其树状结构,这些结构在包封/捕获生物活性成分方面具有独特的潜力。因此,它们在营养、制药和医学科学中迅速获得了有价值的地位。植物化学物质作为生物活性物质的很大一部分,多年来一直受到药理学、医学、食品和化妆品等多个领域学者的研究和应用。但是,溶解度、稳定性和生物利用度问题一直被认为是其应用的限制因素。因此,本研究的主要目的是代表使用树状聚合物作为新型纳米载体来传递植物化学活性化合物,以解决这些问题。因此,在简要回顾了植物化学物质成分之后,本文首先详细解释了树状聚合物,包括定义、类型、代、合成方法和安全问题;然后继续展示了它们在包封植物化学活性化合物和通过树状聚合物主动/被动递药方面的应用。树状聚合物为包封靶向植物化学活性成分提供了广阔而合适的表面。几个参数可以影响树状聚合物的纳米包封产率,包括其代、端基类型、表面电荷、核结构、pH 值和环境因素。树状聚合物的另一个重要问题与它们的毒性有关。阳离子树状聚合物,特别是 PAMAM,通过附着在细胞膜上并干扰其功能,可以对体细胞产生毒性。然而,已经提出了许多解决方案来降低它们的毒性。